Abstract:In order to reduce infection risk of novel coronavirus (SARS-CoV-2), we developed nano-photocatalysts with nanoscale rutile TiO2 (4–8 nm) and CuxO (1–2 nm or less). Their extraordinarily small size leads to high dispersity and good optical transparency, besides large active surface area. Those photocatalysts can be applied to white and translucent latex paints. Although Cu2O clusters involved in the paint coating undergo gradual aerobic oxidation in the dark, the oxidized clusters are re-reduced under > 380… Show more
“…Strontium titanate (SrTiO 3 ) is a cubic perovskite oxide with a bandgap of 3.2 eV and exhibits promising photocatalytic activity in water-splitting reactions. [12][13][14][15][16] In recent decades, powder or nanoscale crystallite forms of TiO 2 [17][18][19][20][21][22][23] and SrTiO 3 [24][25][26][27][28][29][30] have been extensively investigated and have displayed promising photocatalytic performances. These powder and nanocrystalline structures increase the contact area with the solution and the area exposed to solar light; theoretically, PEC activity is also expected to be enhanced with these structures.…”
TiO2 and SrTiO3 are stable and efficient materials for photoelectrochemical (PEC) water splitting. PEC activity is influenced by carrier recombination in crystals of these materials. In this study, we analyzed the effect of dislocations on carrier recombination in TiO2 and SrTiO3 using microwave photoconductive decay measurements on polished and unpolished faces. The apparent slow decay in the unpolished face implies that dislocations trap minority carriers. Based on the different dependences of the injected photon density and temperature, the recombination processes in the polished and unpolished faces differ. A high concentration of oxygen vacancies or hydroxyl in the unpolished face of SrTiO3 was observed by x-ray photoelectron spectroscopy, and dislocations in the unpolished faces of both materials were observed using transmission electron microscopy. Additionally, we found that the photocurrent duration in the unpolished faces was shorter than that in the polished faces for both TiO2 and SrTiO3, confirming that dislocations inhibited photoelectrochemical activity.
“…Strontium titanate (SrTiO 3 ) is a cubic perovskite oxide with a bandgap of 3.2 eV and exhibits promising photocatalytic activity in water-splitting reactions. [12][13][14][15][16] In recent decades, powder or nanoscale crystallite forms of TiO 2 [17][18][19][20][21][22][23] and SrTiO 3 [24][25][26][27][28][29][30] have been extensively investigated and have displayed promising photocatalytic performances. These powder and nanocrystalline structures increase the contact area with the solution and the area exposed to solar light; theoretically, PEC activity is also expected to be enhanced with these structures.…”
TiO2 and SrTiO3 are stable and efficient materials for photoelectrochemical (PEC) water splitting. PEC activity is influenced by carrier recombination in crystals of these materials. In this study, we analyzed the effect of dislocations on carrier recombination in TiO2 and SrTiO3 using microwave photoconductive decay measurements on polished and unpolished faces. The apparent slow decay in the unpolished face implies that dislocations trap minority carriers. Based on the different dependences of the injected photon density and temperature, the recombination processes in the polished and unpolished faces differ. A high concentration of oxygen vacancies or hydroxyl in the unpolished face of SrTiO3 was observed by x-ray photoelectron spectroscopy, and dislocations in the unpolished faces of both materials were observed using transmission electron microscopy. Additionally, we found that the photocurrent duration in the unpolished faces was shorter than that in the polished faces for both TiO2 and SrTiO3, confirming that dislocations inhibited photoelectrochemical activity.
“… 19 Several metal oxide-based photocatalysts, such as CuO 20 and TiO 2, 8 and nanoparticle decorated metal oxides (e.g., Ag/TiO 2 , 21 Au/ZnO, 22 and Pd/TiO 2 8 ) have been used for virus inactivation. In most work reported so far, the reaction is performed in the liquid phase in the presence of a catalyst and virus suspension, 9 , 23 , 24 and there is a lack of knowledge concerning the inactivation mechanism.…”
Titanium dioxide (TiO 2 ) shows significant potential as a self-cleaning material to inactivate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and prevent virus transmission. This study provides insights into the impact of UV-A light on the photocatalytic inactivation of adsorbed SARS-CoV-2 virus-like particles (VLPs) on a TiO 2 surface at the molecular and atomic levels. X-ray photoelectron spectroscopy, combined with density functional theory calculations, reveals that spike proteins can adsorb on TiO 2 predominantly via their amine and amide functional groups in their amino acids blocks. We employ atomic force microscopy and grazing-incidence small-angle X-ray scattering (GISAXS) to investigate the molecular-scale morphological changes during the inactivation of VLPs on TiO 2 under light irradiation. Notably, in situ measurements reveal photoinduced morphological changes of VLPs, resulting in increased particle diameters. These results suggest that the denaturation of structural proteins induced by UV irradiation and oxidation of the virus structure through photocatalytic reactions can take place on the TiO 2 surface. The in situ GISAXS measurements under an N 2 atmosphere reveal that the virus morphology remains intact under UV light. This provides evidence that the presence of both oxygen and UV light is necessary to initiate photocatalytic reactions on the surface and subsequently inactivate the adsorbed viruses. The chemical insights into the virus inactivation process obtained in this study contribute significantly to the development of solid materials for the inactivation of enveloped viruses.
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